Coclaurine structure
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Common Name | Coclaurine | ||
|---|---|---|---|---|
| CAS Number | 486-39-5 | Molecular Weight | 285.338 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 496.9±45.0 °C at 760 mmHg | |
| Molecular Formula | C17H19NO3 | Melting Point | 220-221° | |
| MSDS | N/A | Flash Point | 254.3±28.7 °C | |
Use of CoclaurineCoclaurine is a class of tetrahydroisoquinoline alkaloids isolated from Sarcopetalum harveyanum. Coclaurine is a nicotinic acetylcholine receptor (nAChRs) antagonist[1][2]. |
| Name | (RS)-coclaurine |
|---|---|
| Synonym | More Synonyms |
| Description | Coclaurine is a class of tetrahydroisoquinoline alkaloids isolated from Sarcopetalum harveyanum. Coclaurine is a nicotinic acetylcholine receptor (nAChRs) antagonist[1][2]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 496.9±45.0 °C at 760 mmHg |
| Melting Point | 220-221° |
| Molecular Formula | C17H19NO3 |
| Molecular Weight | 285.338 |
| Flash Point | 254.3±28.7 °C |
| Exact Mass | 285.136505 |
| PSA | 61.72000 |
| LogP | 1.72 |
| Vapour Pressure | 0.0±1.3 mmHg at 25°C |
| Index of Refraction | 1.621 |
| InChIKey | LVVKXRQZSRUVPY-HNNXBMFYSA-N |
| SMILES | COc1cc2c(cc1O)C(Cc1ccc(O)cc1)NCC2 |
| Hazard Codes | Xi |
|---|
| Precursor 0 | |
|---|---|
| DownStream 1 | |
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Name: Inhibition of dopamine transporter-mediated [3H]dopamine uptake in Wistar rat striata...
Source: ChEMBL
Target: Sodium-dependent dopamine transporter
External Id: CHEMBL952559
|
|
Name: Ratio of IC50 for rat striatum dopamine D2 receptor to IC50 for Wistar rat striatal s...
Source: ChEMBL
Target: N/A
External Id: CHEMBL952561
|
|
Name: Ratio of IC50 for rat striatum dopamine D1 receptor to IC50 for Wistar rat striatal s...
Source: ChEMBL
Target: N/A
External Id: CHEMBL952560
|
| (1S)-1-(4-Hydroxybenzyl)-6-methoxy-1,2,3,4-tetrahydro-7-isoquinolinol |
| Coclaurine |
| 1-(4-Hydroxybenzyl)-6-methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol |
| 1-(4-Hydroxybenzyl)-6-methoxy-1,2,3,4-tetrahydro-7-isoquinolinol |
| Machiline |
| 1-(p-Hydroxybenzyl)-6-methoxy-7-hydroxy-1,2,3,4-tetrahydroisoquinoline |
| 1,2,3,4-Tetrahydro-1-(p-hydroxybenzyl)-6-methoxy-7-isoquinolinol |
| 6-Methoxy-7-hydroxy-(1R)-[(4-hydroxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline |